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Clinical goniometer, manually-operated - ARTG 474971

Access comprehensive regulatory information for Clinical goniometer, manually-operated in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 474971 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by DePuy Ireland UC in Ireland. The device registration started on January 03, 2025.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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TGA ARTG Official Data
Class I
ARTG 474971
Class I
Clinical goniometer, manually-operated
ARTG ID: 474971
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Clinical goniometer, manually-operated
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Intended Purpose

A reusable manually-operated device that is used to measure the range of motion of the limb of a patient by measuring the angle of movement achieved at the joint.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
474971
Start Date
January 03, 2025
Effective Date
January 03, 2025
Manufacturer
Country
Ireland
Address
Loughbeg Ringaskiddy, Co Cork